JP2023524262A - Synthesis of sulfonamide intermediates - Google Patents

Abstract

Provided herein are methods of synthesizing Mcl-1 inhibitors and intermediates, such as compound Z, that can be used to prepare the Mcl-1 inhibitors. Specifically, provided herein are methods of synthesizing Compound A1 and salts or solvates thereof, and Compound A2 and salts and solvates thereof. TIFF2023524262000057.tif86170

Description

CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Patent Application No. 63/020,951, filed May 6, 2020, which is hereby incorporated by reference. is incorporated herein by reference in its entirety for all purposes as if fully set forth in .

The present disclosure provides (1S,3′R,6′R,7′S,8′E,11′S,12′R)-6-chloro-7′-methoxy-11′,12′-dimethyl-3 ,4-dihydro-2H,15′H-spiro[naphthalene-1,22′[20]oxa[13]thia[1,14]diazatetracyclo[14.7.2.0 ^3,6 . 0 ^19,24 ]pentacosa[8,16,18,24]tetraen]-15′-one 13′,13′-dioxide (Compound A1; AMG 176), preparation of salts or solvates thereof, and (1S, 3′R,6′R,7′R,8′E,11′S,12′R)-6-chloro-7′-methoxy-11′,12′-dinethyl-7′-(( 9aR)-octahydro-2H-pyrido[1,2-a]pyrazin-2-ylmethyl)-3,4-dihydro-2H,15′H-spiro[naphthalene-1,22′-[20]oxa[13] thia[1,14]diazatetracyclo[14.7.2.0 ^3,6 . 0 ^19,24 ]pentacosa[8,16,18,24]tetraen]-15′-one 13′,13′-dioxide (Compound A2; AMG 397), an intermediate useful in the preparation of salts or solvates thereof It relates to a method for synthesizing These compounds are inhibitors of myeloid cell leukemia 1 protein (Mcl-1).

は、骨髄細胞白血病１（Ｍｃｌ－１）の阻害剤として有用である。 Compound (1S,3′R,6′R,7′S,8′E,11′S,12′R)-6-chloro-7′-methoxy-11′,12′-dimethyl-3,4- Dihydro-2H,15′H-spiro[naphthalene-1,22′[20]oxa[13]thia[1,14]diazatetracyclo[14.7.2.0 ^3,6 . 0 ^19,24 ]pentacosa[8,16,18,24]tetraen]-15′-one 13′,13′-dioxide (compound A1):

is useful as an inhibitor of myeloid cell leukemia 1 (Mcl-1).

は、骨髄細胞白血病１（Ｍｃｌ－１）の阻害剤として有用である。 Compound (1S,3′R,6′R,7′R,8′E,11′S,12′R)-6-chloro-7′-methoxy-11′,12′-dineethyl-7′-( (9aR)-octahydro-2H-pyrido[1,2-a]pyrazin-2-ylmethyl)-3,4-dihydro-2H,15′H-spiro[naphthalene-1,22′-[20]oxa[13 ]thia[1,14]diazatetracyclo[14.7.2.0 ^3,6 . 0 ^19,24 ]pentacosa[8,16,18,24]tetraen]-15′-one 13′,13′-dioxide (compound A2):

is useful as an inhibitor of myeloid cell leukemia 1 (Mcl-1).

One common characteristic of human cancers is the overexpression of Mcl-1. Mcl-1 overexpression prevents cancer cells from undergoing programmed cell death (apoptosis), allowing cells to survive despite extensive genetic damage.

Mcl-1 is a member of the Bcl-2 family of proteins. The Bcl-2 family includes pro-apoptotic members such as BAX and BAK, which upon activation form homo-oligomers in the outer mitochondrial membrane, which are the steps leading to apoptosis, pore formation and mitochondrial content. lead to deviance. Anti-apoptotic members of the Bcl-2 family (eg, Bcl-2, Bcl-XL, and Mcl-1) block the activity of BAX and BAK. Other proteins (eg, BID, BIM, BIK, and BAD) exhibit additional regulatory functions. Studies have shown that Mcl-1 inhibitors may be useful for the treatment of cancer. Mcl-1 is overexpressed in many cancers.

US Pat. No. 9,562,061, which is incorporated herein by reference in its entirety, discloses Compound A1 as a Mcl-1 inhibitor and provides methods for its preparation. However, improved synthetic methods that provide higher yields and purities of compound A1 are desired, especially for the commercial production of compound A1.

US Pat. No. 10,300,075, which is incorporated herein by reference in its entirety, discloses compound A2 as a Mcl-1 inhibitor and provides methods for its preparation. However, improved synthetic methods that provide higher yields and purities of compound A2 are desirable, especially for the commercial production of compound A2.

又はその塩を合成する方法であって、（ａ）（２Ｓ，３Ｓ）－ブタン－２，３－ジオール、臭化物源、及び酢酸を混合して、化合物Ｉ

を形成すること；（ｂ）化合物Ｉ、及び非求核塩基を混合して、化合物Ｊ

を形成すること；（ｃ）化合物Ｊ、及びアリル求核試薬を混合して、化合物Ｋ

を形成すること；（ｄ）化合物Ｋ、脱離基試薬、及びアミン塩基を混合して、化合物Ｌ

を形成することであり、式中、ＬＧは、脱離基である、形成すること；（ｅ）化合物Ｌ、非求核塩基、及びＡｒ^１－ＳＨを混合して、化合物Ｍ

を形成することであり、式中、Ａｒ^１は、Ｏ、Ｎ、及びＣから選択される１～３個の環ヘテロ原子を含む５～１２員のヘテロアリールである、形成すること；（ｆ）化合物Ｍを酸化させて、化合物Ｎ

を形成すること；並びに（ｇ）化合物Ｎ、塩基、及びヒドロキシルアミン－Ｏ－スルホン酸を混合して、化合物Ｚを形成することを含む方法である。 Provided herein are compounds Z

or a method of synthesizing a salt thereof, comprising mixing (a) (2S,3S)-butane-2,3-diol, a bromide source, and acetic acid to form compound I

(b) combining compound I and a non-nucleophilic base to form compound J

(c) combining compound J and an allyl nucleophile to form compound K

(d) mixing compound K, a leaving group reagent, and an amine base to form compound L

(e) combining compound L, a non-nucleophilic base, and Ar ¹ —SH to form compound M

( ^f ) oxidizing compound M to compound N

and (g) combining compound N, a base, and hydroxylamine-O-sulfonic acid to form compound Z.

を合成することを含む方法である。 Also provided herein are Compounds A1 or salts or solvates thereof, or Compounds A2 or salts or solvates thereof, using Compound Z:

is a method comprising synthesizing the

Further aspects and advantages will be apparent to those skilled in the art from a review of the detailed description below. With the understanding that this disclosure is illustrative and is not intended to limit the invention to the specific embodiments described herein, the following description herein Including specific embodiments.

Provided herein are methods of synthesizing Mcl-1 inhibitors and corresponding sulfonamide Mcl-1 inhibitor intermediates. Specifically, this sulfonamide intermediate is converted to (1S,3′R,6′R,7′S,8′E,11′S,12′R)-6-chloro-7′-methoxy-11 ',12'-dimethyl-3,4-dihydro-2H,15'H-spiro[naphthalene-1,22'[20]oxa[13]thia[1,14]diazatetracyclo[14.7.2 .0 ^3,6 . 0 ^19,24 ]pentacosa[8,16,18,24]tetraen]-15′-one 13′,13′-dioxide (Compound A1) or a salt or solvate thereof, and (1S,3 'R,6'R,7'R,8'E,11'S,12'R)-6-chloro-7'-methoxy-11',12'-dineethyl-7'-((9aR)-octahydro -2H-pyrido[1,2-a]pyrazin-2-ylmethyl)-3,4-dihydro-2H,15′H-spiro[naphthalene-1,22′-[20]oxa[13]thia[1, 14] diazatetracyclo[14.7.2.0 ^3,6 . 0 ^19,24 ]pentacosa[8,16,18,24]tetraen]-15′-one 13′,13′-dioxide (Compound A2) or a salt or solvate thereof may be used in a method to synthesize:

US Pat. No. 9,562,061, which is incorporated herein by reference in its entirety, discloses Compound A1 or its salts or solvates as Mcl-1 inhibitors, and preparing these A method is also provided. US Pat. No. 9,562,061 also discloses methods for synthesizing the sulfonamide Mcl-1 inhibitor intermediates used in the synthesis of compound A1.

US Pat. No. 10,300,075, which is incorporated herein by reference in its entirety, discloses Compound A2 or its salts or solvates as Mcl-1 inhibitors, and preparing these A method is also provided. US Pat. No. 10,300,075 also discloses a method for synthesizing the sulfonamide Mcl-1 inhibitor intermediates used in the synthesis of compound A2.

を合成するプロセスが説明されている。 Specifically, in the '061 patent, the sulfonamide intermediate compound Z, shown in Scheme 1:

is described.

’０６１号特許では、合成の次の工程での使用前での中間体化合物のそれぞれの単離が説明されている。さらに、’０６１号特許では、（４Ｓ，５Ｓ）－４，５－ジメチル－１，３，２－ジオキサチオラン ２，２－ジオキシドから（２Ｓ，３Ｓ）－３－メチルヘキサ－５エン－２－オールへの工程により、化学純度及びキラル純度のレベルが変動するという合成結果となり、そのため、クロマトグラフィー等の面倒の後処理工程が必要となる可能性があり、結果として収率が大幅に低下する。有利なことに、本明細書で説明されている出発ブタンジオールからの異なる合成戦略の使用により、結晶性中間体（例えば、化合物Ｎ、Ａｒ^１＝ピリジル又はピリミジニル）及び結晶性標的化合物（Ｚ）の単離によって、収率が高くなり、効率がよくなり、且つ高純度の生成物が生成される。本明細書で説明されている方法は、除去することが困難な二量体硫黄系不純物の形成を回避し、化学純度及びキラル純度を改善し、安全性を改善し、且つ小規模（例えば１グラム未満）及び大規模（例えば数ｋｇ）の両方で製造するため柔軟性をもたらす。 Scheme 1 - Synthesis of sulfonamide Mcl-1 inhibitor intermediates from the '061 patent

The '061 patent describes isolation of each of the intermediate compounds prior to use in the next step of the synthesis. Further, in the '061 patent, (4S,5S)-4,5-dimethyl-1,3,2-dioxathiolane 2,2-dioxide to (2S,3S)-3-methylhex-5en-2-ol The step of results in syntheses with varying levels of chemical and chiral purity, which may require cumbersome work-up steps such as chromatography, resulting in significantly lower yields. Advantageously, by using different synthetic strategies from the starting butanediol described herein, a crystalline intermediate (e.g. compound N, Ar ¹ =pyridyl or pyrimidinyl) and a crystalline target compound (Z) provides high yields, efficiencies, and high purity products. The methods described herein avoid the formation of dimeric sulfur impurities that are difficult to remove, improve chemical and chiral purity, improve safety, and are small scale (e.g., 1 Provides flexibility to manufacture both on a scale of less than a gram) and on a large scale (eg several kg).

又はその塩を合成する方法であって、
（ａ）（２Ｓ，３Ｓ）－ブタン－２，３－ジオール、臭化物源、及び酢酸を混合して、化合物Ｉ

を形成すること；
（ｂ）化合物Ｉ、及び非求核塩基を混合して、化合物Ｊ

を形成すること；
（ｃ）化合物Ｊ、及びアリル求核試薬を混合して、化合物Ｋ

を形成すること；
（ｄ）化合物Ｋ、脱離基試薬、及びアミン塩基を混合して、化合物Ｌ

を形成することであり、式中、ＬＧは、脱離基である、形成すること、
（ｅ）化合物Ｌ、非求核塩基、及びＡｒ^１－ＳＨを混合して、化合物Ｍ

を形成することであり、式中、Ａｒ^１は、Ｏ、Ｎ、及びＳから選択される１～３個の環ヘテロ原子を含む５～１２員のヘテロアリールである、形成すること；
（ｆ）化合物Ｍを酸化させて、化合物Ｎ

を形成すること；
（ｇ）化合物Ｎ、塩基、及びヒドロキシルアミン－Ｏ－スルホン酸を混合して、化合物Ｚを形成することを含む方法である。 Provided herein is compound Z:

Or a method for synthesizing a salt thereof,
(a) (2S,3S)-butane-2,3-diol, a bromide source, and acetic acid are mixed to form compound I

forming;
(b) compound I and a non-nucleophilic base are mixed to form compound J;

forming;
(c) compound J and an allyl nucleophile are mixed to form compound K;

forming;
(d) Compound K, a leaving group reagent, and an amine base are mixed to form Compound L;

wherein LG is a leaving group;
(e) combining compound L, a non-nucleophilic base, and Ar ¹ —SH to form compound M;

wherein Ar ¹ is a 5-12 membered heteroaryl containing 1-3 ring heteroatoms selected from O, N, and S;
(f) oxidizing compound M to compound N

forming;
(g) combining compound N, a base, and hydroxylamine-O-sulfonic acid to form compound Z;

A general reaction scheme for the methods described herein is shown in Scheme 2 below.
Scheme 2: Overall process for the synthesis of sulfonamide Mcl-1 inhibitor intermediates

Bromination and acetylation of 2S,3S-butane-diol to form compound I (step (a))
The method of the present disclosure involves bromination and acetylation of 2S,3S-butane-diol to obtain compound I, which converts 2S,3S-butane-diol, a bromide source, and acetic acid Including mixing.

The term "bromide source" as used herein refers to the bromide source used to replace the hydroxyl group on the butane-diol. In some embodiments, the bromide source herein comprises HBr, _PBr3 , or combinations thereof. In some embodiments, the bromide source herein comprises HBr.

In some embodiments, the bromide source is provided in acetic acid solution. In some embodiments, the bromide source may be present in acetic acid in an amount of 20% w/w to 50% w/w. For example, the bromide source may be present in acetic acid in an amount of 25 w/w% to 40 w/w%, 25 w/w% to 35 w/w%, or 30 w/w% to 35 w/w%, such as 20 w/w /w%, 25 w/w%, 30 w/w%, 32 w/w%, 33 w/w%, 34 w/w%, 35 w/w%, 40 w/w%, 45 w/w%, or 50 w/w% may be present in the acetic acid. In some embodiments, HBr may be present in acetic acid. In some embodiments, HBr may be present as a 33 w/w % solution in acetic acid.

The 2S,3S-butane-diol and bromide source may be present in a molar ratio of 1:1 to 1:6, such as a minimum of 1:1, 1.05, 1:1.2, 1:1.5. , 1:1.75, 1:2, 1:2.25, 1:2.5, 1:3, 1:4 and/or up to 1:6, 1:5, 1:4 , 1:3, 1:2.75, 1:2.5, 1:2.25, 1:2, or 1:1.5 molar ratios, for example from 1:1 to 1:3 .5, 1:2 to 1:4, 1:2 to 1:5, or 1:1.5 to 1:3.5 molar ratios. In some embodiments, the molar ratio of Compound I to non-nucleophilic base is 1:3.5.

Bromination of butanediol can be carried out at a temperature of −20° C. to 10° C., for example a minimum of −20, −15, −10, −5, 0, 5, or 10 and/or a maximum of 10, 5 , 0, or -10°C, such as -15°C to 10°C, -10°C to 10°C, -5°C to 10°C, or 0°C to 10°C. In some embodiments, this bromination is performed at a temperature of 10°C.

In some embodiments, the mixing of step (a) can be performed for 1 hour to 24 hours. In some embodiments, the mixing of step (a) may be performed for 15 hours to 20 hours, or 10 hours to 24 hours, or 12 hours to 24 hours, or 14 hours to 21 hours. For example, the mixing of step (a) can be for 1 hour, 5 hours, 10 hours, 12 hours, 15 hours, 16 hours, 17 hours, 18 hours, 19 hours, 20 hours, or 24 hours.

Bromination/acetylation of butanediol affords compound I which can be processed directly to the next step without the need for substantial purification. As used herein, the term "substantially purified" refers to any purification method other than solvent washing and/or distillation, such as chromatography (e.g. column chromatography), crystallization, filtration, or any combination thereof. In embodiments, neutralization of any acid (e.g., acetic acid and/or HBr) remaining in the formation of compound I may be achieved by mixing with a base such as potassium carbonate in water, compound I is converted to tert - can be extracted with an organic solvent such as butyl methyl ether (MTBE). In embodiments, the extracted Compound I may be used in step (b) described below, or may be used after removal of the solvent used for extraction (eg "solvent free").

In some embodiments where compound I is processed directly to the next step, compound I may be provided in a solution comprising an organic solvent. Organic solvents are well known in the art. Non-limiting examples of contemplated organic solvents include acetonitrile, toluene, benzene, xylene, chlorobenzene, fluorobenzene, naphthalene, benzotrifluoride, tetrahydrofuran (THF), tetrahydropyran, dimethylformamide (DMF), tetrahydrofurfuryl alcohol. , diethyl ether, dibutyl ether, diisopropyl ether, dimethyl tert-butyl ether (MTBE), 2-methyltetrahydrofuran (2-MeTHF), dimethylsulfoxide (DMSO), 1,2-dimethoxyethane (1,2-DME), 1, 2-dichloroethane (1,2-DCE), 1,4-dioxane, cyclopentyl methyl ether (CPME), chloroform, carbon tetrachloride, dichloromethane (DCM), methanol, ethanol, propanol, and 2-propanol. In some embodiments, the organic solvent comprises MTBE. The organic solvent may be present in an amount from 0.1 L/kg 2S,3S-butane-diol to 10 L/kg 2S,3S-butane-diol, such as a minimum of 0.5, 1, 1.5 , 2, 3, 5, 7.5, or 10 L/kg of 2S,3S-butane-diol, and/or up to 10, 7.5, 5, 3.5, 1.5, or 0.5 L/kg may be present in amounts of kg 2S,3S-butane-diol, such as 1-4 L/kg 2S,3S-butane-diol, 1.5-10 L/kg 2S,3S-butane-diol, or 5 L /kg to 10 L/kg of 2S,3S-butane-diol.

の構造を有する。 Epoxidation of compound I to form compound J (step (b))
The methods of the disclosure may include epoxidation of compound I to obtain compound J. The methods herein can include synthesizing compound J by combining compound I and a non-nucleophilic base to form compound J. As provided herein, compound J is

has the structure

A non-nucleophilic base, as used herein, can be any suitable non-nucleophilic base known to those of skill in the art. Contemplated non-nucleophilic bases include, for example, lithium hexamethyldisilazide (“HMDS”), sodium HMDS, potassium HMDS, lithium diisopropylamide, sodium diisopropylamide, potassium diisopropylamide, lithium tert- butoxide, sodium tert-butoxide, potassium tert-butoxide, lithium tert-amylate, sodium tert-amylate, potassium tert-amylate, 2,2,6,6-tetramethylpiperidine (TMP), LiTMP, 1,1,3, 3-tetramethylguanidine (TMG), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), 1,5-diazabicyclo[4.3.0]non-5-ene, and these any combination of In some embodiments, the non-nucleophilic base comprises lithium tert-butoxide, sodium tert-butoxide, potassium tert-butoxide, or combinations thereof. In some embodiments, the non-nucleophilic base is potassium tert-butoxide. In some embodiments, the non-nucleophilic base is sodium tert-butoxide. In some embodiments, the non-nucleophilic base is sodium tert-amylate. In some embodiments, the non-nucleophilic base is potassium tert-amylate.

Compound I and the non-nucleophilic base may be present in a molar ratio of 1:1 to 1:5, for example a minimum of 1:1, 1.05, 1:1.2, 1:1.5, 1: molar ratios of 1.75, 1:2, 1:2.25, 1:2.5, 1:3, 1:4 and/or up to 1:5, 1:4, 1:3, 1: may be present in a molar ratio of 2.75, 1:2.5, 1:2.25, 1:2, or 1:1.5, for example from 1:1 to 1:2.5, from 1:1 to It can be present in molar ratios of 1:3, 1:1 to 1:4, 1:1.25 to 1:3, or 1:1.1 to 1:2.5. In some embodiments, the molar ratio of Compound I to non-nucleophilic base is 1:2.5.

In some embodiments, step (b) further comprises monoethylene glycol. In some embodiments, step (b) comprises monoethylene glycol and potassium tert-butoxide. In some embodiments, step (b) comprises monoethylene glycol and sodium tert-butoxide.

Monoethylene glycol may be present in an amount of 2 L/kg of Compound I to 5 L/kg of Compound I, such as a minimum of 2, 2.5, 3, 5 L/kg of Compound I, and/or a maximum of 5 L/kg of Compound I. , 3.5, or 3 L/kg of Compound I, for example, 2-4 L/kg of Compound I, 2.5-5 L/kg of Compound I, or 3 L/kg-4 L/kg of Compound I. Compound I can be present in amounts.

In some embodiments, the mixing of step (b) can be performed in an organic solvent. In some embodiments, the organic solvent comprises tert-butyl methyl ether, 2-methyltetrahydrofuran, cyclopentyl methyl ether, dimethoxyethane, or combinations thereof. In some embodiments, the organic solvent comprises tert-butyl methyl ether.

In some embodiments, the monoethylene glycol and non-nucleophilic base are mixed together prior to mixing with Compound I. This mixing of the monoethylene glycol and the non-nucleophilic base may be carried out such that the non-nucleophilic base is added to the monoethylene glycol in such a way that the temperature of the resulting mixture is maintained between 20°C and 40°C. In some embodiments, the non-nucleophilic base is added to monoethylene glycol over 3-7 hours or over 4-6 hours. After all the non-nucleophilic bases have been added to the monoethylene glycol, the mixture is subjected to a temperature of 70-120° C. under reduced pressure (eg, a pressure of 400 mmHg) to produce a by-product of protonated non-nucleophilic bases. (eg, t-butanol is produced when the non-nucleophilic base is t-butoxide) can be removed, leaving the deprotonated monoethylene glycol. Compound I is then added to the deprotonated monoethylene glycol at a temperature of 20° C. to 40° C. (eg 30° C.) for 15 minutes to 120 minutes (eg 15 minutes to 60 minutes, or 30 minutes). ) can be mixed. In some embodiments, the resulting epoxide, compound J, can be isolated by distillation from the reaction mixture.

Epoxidation of compound I gives compound J which can be processed directly to the next step without the need for isolation.

の構造を有する。 Allyl Addition to Compound J to Form Compound K (Step (C))
The method of the present disclosure involves allyl addition to compound J to give compound K. The methods herein can include synthesizing compound K by mixing compound J and an allyl nucleophile to form compound K. As provided herein, compound K is

has the structure

の構造を有しており、式中、Ｘ^１は、ＭｇＣｌ、ＭｇＢｒ、ＭｇＩ、Ｌｉ、ＣｕＬｉ、ＺｎＸ^３、Ｉｎ（Ｉ）、又はＩｎ（Ｘ^２）_２であり；それぞれのＸ^２は、独立して、Ｃｌ、Ｂｒ、又はＩであり、Ｘ^３は、Ｃｌ、Ｂｒ、Ｉ、ＯＴｆ、ＯＴｓ、ＯＡｃ、又はａｃａｃである。一部の実施形態では、Ｘ^１は、ＭｇＣｌ、ＭｇＢｒ、又はＭｇＩである。一部の実施形態では、Ｘ^１は、ＭｇＣｌである。一部の実施形態では、Ｘ^１は、ＭｇＢｒ又はＭｇＩである。 Allyl nucleophiles are

where X ¹ is MgCl, MgBr, MgI, Li, CuLi, ZnX ³ , In(I), or In(X ² ) ₂ ; each X ² independently is Cl, Br, or I, and ^X3 is Cl, Br, I, OTf, OTs, OAc, or acac. In some embodiments, X ¹ is MgCl, MgBr, or MgI. In some embodiments, X ¹ is MgCl. In some embodiments, X ¹ is MgBr or MgI.

In some embodiments, X ¹ is Li. In some embodiments, X ¹ is CuLi.

In embodiments, X ¹ is ZnX ³ , wherein X ³ is Cl, Br, I, OTf, OTs, OAc, or acac. In some embodiments, X ¹ is ZnCl or ZnBr. In some embodiments, X ¹ is ZnCl. In some embodiments, X ¹ is ZnBr. In some embodiments, X ¹ is ZnOTf or ZnOTs. In some embodiments, X ¹ is ZnOAc or Zn(acac). In some embodiments, X ¹ is In(I), or InCl, or InBr, or InI.

Compound J and the allyl nucleophile may be present in a molar ratio of 1:1.05 to 1:3, such as a minimum of 1:1, 1.05, 1:1.2, 1:1.5, molar ratios of 1:1.75, 1:2, 1:2.25, 1:2.5 and/or up to 1:3, 1:2.75, 1:2.5, 1:2. may be present in molar ratios of 25, 1:2, or 1:1.5, for example 1:1 to 1:2.5, 1:1 to 1:2, 1:1 to 1:3, 1: It may be present in a molar ratio of 1.25 to 1:2, or 1:1.1 to 1:3. In some embodiments, the molar ratio of compound J to allyl nucleophile is 1:1.2.

In some embodiments, the allyl addition, step (c), mixing may be performed in an organic solvent. In some embodiments, the organic solvent comprises tetrahydrofuran (THF), 2-methyltetrahydrofuran, tert-butylmethylether (MTBE), cyclopentylmethylether, dimethoxyethane, or combinations thereof. In some embodiments, the organic solvent comprises tert-butyl methyl ether. In some embodiments, the organic solvent comprises THF. In some embodiments, the organic solvent includes THF and MTBE.

In some embodiments, compound J can be added dropwise to an allyl nucleophile. In some embodiments, compound J is added dropwise to the allyl nucleophile over 1 hour to about 5 hours, such as 1 hour, 2 hours, 3 hours, 4 hours, or 5 hours. In some embodiments, compound J is added dropwise to the allyl nucleophile over 3 hours.

In some embodiments, after combining Compound J and the allyl nucleophile, the two are mixed for 1 hour to 6 hours, such as 1 hour, 1.5 hours, 2 hours, 2.5 hours. , 3 hours, 3.5 hours, 4 hours, 5 hours, or 6 hours. In some embodiments, the mixing of step (c) is performed for 3 hours.

The mixing of step (C) can be carried out at a temperature of -20°C to 10°C, for example at least -20, -15, -10, -5, 0, 5, or 10 and/or at most It can be carried out at a temperature of 10, 7, 5, 0, or -10, for example -15°C to 10°C, -10°C to 10°C, -5°C to 10°C, 0°C to 10°C, or 7°C to It can be done at a temperature of 10°C. In some embodiments, this mixing is performed at a temperature of 7°C to 10°C.

In some embodiments, the reaction of compound J with an allyl nucleophile can be quenched by adding an aqueous solution of citric acid.

This allyl addition affords compound K which can be processed directly to the next step without the need for substantial purification.

の構造を有しており、式中、ＬＧは、脱離基である。 Leaving group addition to compound K to form compound L (step (d))
The method of the present disclosure involves leaving group (LG) addition to compound K to give compound L. The methods herein can include synthesizing compound L by combining compound K, a leaving group reagent, and an amine base to form compound L. As provided herein, compound L is

where LG is a leaving group.

Compound K is reacted with a leaving group reagent and an amine base, which converts the hydroxyl group of compound K to a leaving group to form compound L. A leaving group, as used herein, refers to any suitable atom or functional group that can be displaced by a nucleophile during a nucleophilic substitution. Leaving group reagents that can convert a hydroxyl group into a leaving group to favor nucleophilic substitution are known in the art. Non-limiting examples of suitable leaving groups include halides (eg F, Cl, Br, or I), or sulfonyl.

を指しており、式中、Ｒ－Ｏは、脱離基に変換されているヒドロキシル基に由来しており、ＬＧ’は、スルホニル脱離基の残りに由来している。一部の実施形態では、スルホニル脱離基は、メシル、トシル、ノシル、及びトリフリルからなる群から選択される。一部の実施形態では、スルホニル脱離基は、メシルを含む。 In some embodiments, LG is a sulfonyl leaving group. As used herein, the term "sulfonyl leaving group" refers to a leaving group -

wherein RO is from the hydroxyl group that has been converted to a leaving group and LG' is from the remainder of the sulfonyl leaving group. In some embodiments, the sulfonyl leaving group is selected from the group consisting of mesyl, tosyl, nosyl, and triflyl. In some embodiments, the sulfonyl leaving group includes mesyl.

Generally, the leaving group reagent can be any suitable leaving group reagent known to those skilled in the art that is used to convert a hydroxyl group to a leaving group. In some embodiments, the leaving group reagent can include mesyl chloride.

Compound K and the leaving group reagent may be present in a molar ratio of 1:1.2 to 1:2, such as a minimum molar ratio of 1:1.2, 1:1.5, 1:1.6. , and/or may be present in a molar ratio of up to 1:2, 1:1.75, 1:1.5, such as 1:1.2 to 1:1.9, 1:1.2 to 1 :7, or in a molar ratio of 1:1.2 to 1:1.5. In some embodiments, the molar ratio of Compound K to leaving group reagent is 1:1.4.

Combining in step (d) can include an amine base (eg, mono-, di-, or trialkylamine, substituted or unsubstituted piperidine, substituted or unsubstituted pyridine). In some embodiments, the amine base is pyridine, trimethylamine, triethylamine, aniline, diisopropylethylamine, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), 1,4-diazabicyclo[ 2.2.2] octane (DABCO), 2,6-lutidine, or combinations thereof. In some embodiments, the amine base is triethylamine.

Compound K and amine base may be present in a molar ratio of 1:1.8 to 1:3.3, such as a minimum molar ratio of 1:1.8, 1:2, 1:2.5, and /or may be present in molar ratios up to 1:3.3, 1:3, 1:2.5, such as from 1:1.8 to 1:3, from 1:2 to 1:3, or 1: It can be present in a molar ratio of 2-1:2.5. In some embodiments, the molar ratio of Compound K to leaving group reagent is 1:2.3.

In some embodiments, the mixing of step (d), the leaving group addition, can be performed in an organic solvent comprising dichloromethane, tetrahydrofuran, 2-methyltetrahydrofuran, tert-butyl methyl ether, or combinations thereof. . In some embodiments, the organic solvent comprises tert-butyl methyl ether. In some embodiments, the organic solvent comprises THF. In some embodiments, the organic solvent does not contain dichloromethane.

In some embodiments, the leaving group reagent can be slowly added to the solution of Compound K and the amine base. In some embodiments, the leaving group reagent is added to the solution of Compound K and the amine base over 2-3 hours, such as over 2 hours, 2.5 hours, or 3 hours. . In some embodiments, the leaving group reagent is added to the solution of Compound K and the amine base over 2-3 hours and then stirred for 10 minutes-1 hour. In some embodiments, a leaving group reagent is added to a solution of Compound K and an amine base over 2.5 hours. In some embodiments, a leaving group reagent is added to a solution of Compound K and an amine base over 2.5 hours and then stirred for 30 minutes.

The mixing of step (d) may be performed at a temperature of -10°C to 10°C, such as a minimum of -10, -5, 0, or 5, and/or a maximum of 10, 7, 5, 0, Alternatively, it can be carried out at a temperature of -10°C, for example at a temperature of -10°C to 5°C, -10°C to 0°C, -5°C to 10°C, 0°C to 10°C. In some embodiments, this mixing is performed at a temperature of 5°C.

This leaving group addition affords compound L, which can be processed directly to the next step without the need for substantial purification.

の構造を有しており、式中、Ａｒ^１は、Ｏ、Ｎ、及びＳから選択される１～３個の環ヘテロ原子を含む５～１２員のヘテロアリールである。 Nucleophilic substitution of compound L to form compound M (step (e))
The method of the present disclosure involves nucleophilic substitution of compound L to give compound M. The methods herein involve synthesizing compound M by mixing compound L, a non-nucleophilic base, and Ar ¹ —SH to form compound M. As provided herein, compound M is

wherein Ar ¹ is a 5-12 membered heteroaryl containing 1-3 ring heteroatoms selected from O, N, and S.

As used herein, the term "heteroaryl" refers to a cyclic aromatic ring having a total of 5-12 ring atoms (eg, a monocyclic aromatic ring having a total of 5-6 ring atoms). refers to a cyclic aromatic ring containing from 1 to 3 heteroatoms selected from nitrogen, oxygen and sulfur in the aromatic ring. Unless otherwise indicated, a heteroaryl group can be unsubstituted or have one or more (especially 1 to 4) substituents such as halo, alkyl, alkenyl, OCF ₃ , It may be substituted with substituents selected from _NO2 , CN, NC, OH, alkoxy, amino, _CO2H , _CO2alkyl , aryl, and heteroaryl. The heteroaryl group is optionally substituted with one or more of alkyl and alkoxy groups. The heteroaryl group can be isolated (e.g. pyridyl) or another heteroaryl group (e.g. purinyl), a cycloalkyl group (e.g. tetrahydroquinolinyl), a heterocycloalkyl group (e.g. dihydronaphthyridinyl), and/ or fused to aryl groups such as benzothiazolyl and quinolyl. Examples of heteroaryl groups include, but are not limited to: thienyl, furyl, pyridyl, pyrrolyl, oxazolyl, quinolyl, thiophenyl, isoquinolyl, indolyl, triazinyl, triazolyl, isothiazolyl, isoxazolyl, imidazolyl, benzothiazolyl, pyrazinyl, pyrimidinyl. , thiazolyl, and thiadiazolyl. When a heteroaryl group is fused to another heteroaryl group, each ring can have a total of 5 or 6 ring atoms and 1-3 heteroatoms in the aromatic ring.

からなる群から選択される。一部の実施形態では、Ａｒ^１は、

である。 In some embodiments, Ar ¹ is

selected from the group consisting of In some embodiments, Ar ¹ is

is.

Compound L and Ar ¹ -SH may be present in a molar ratio of 1:1.05 to 1:2.5, such as a minimum of 1:1.05, 1:1.25, 1:1.5, may be present in a molar ratio of 1:1.6 and/or up to a molar ratio of 1:2.5, 1:2, 1:1.75, 1:1.5, for example 1:1.05 It may be present in a molar ratio of ˜1:2.25, 1:1.1 to 1:2, or 1:1.05 to 1:1.2. In some embodiments, the molar ratio of compound L to Ar ¹ -SH is 1:1.08.

A non-nucleophilic base, as used herein, can be any suitable non-nucleophilic base known to those of skill in the art. Suitable non-nucleophilic bases may include, for example, lithium hexamethyldisilazide (“HMDS”), sodium HMDS, potassium HMDS, lithium diisopropylamide, sodium diisopropylamide, potassium diisopropylamide, lithium tert-butoxide. , sodium tert-butoxide, potassium tert-butoxide, lithium tert-amylate, sodium tert-amylate, potassium tert-amylate, 2,2,6,6-tetramethylpiperidine (TMP), LiTMP, 1,1,3,3 -tetramethylguanidine (TMG), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), 1,5-diazabicyclo[4.3.0]non-5-ene, and these Any combination. In some embodiments, the non-nucleophilic base is lithium hexamethyldisilazide (“HMDS”), sodium HMDS, potassium HMDS, lithium diisopropylamide, sodium diisopropylamide, potassium diisopropylamide, lithium tert-butoxide, sodium tert -butoxide, potassium tert-butoxide, lithium tert-amylate, sodium tert-amylate, potassium tert-amylate, or combinations thereof. In some embodiments, the non-nucleophilic base comprises sodium tert-butoxide, potassium tert-butoxide, or sodium tert-amylate.

Compound L and non-nucleophilic base may be present in a molar ratio of 1:1.1 to 1:4, such as a minimum of 1:1.1, 1:1.2, 1:1.5, 1: 2, 1:2.5 and/or up to a molar ratio of 1:4, 1:3.5, 1:3, 1:2.5, for example 1:1.1 It may be present in a molar ratio of ~1:3, 1:1.1 to 1:2, or 1:1.1 to 1:1.3. In some embodiments, the molar ratio of compound L to non-nucleophilic base is 1:1.2.

In some embodiments, the mixing of step (e) can be performed in an organic solvent comprising tetrahydrofuran, 2-methyltetrahydrofuran, tert-butyl methyl ether, toluene, or combinations thereof. In some embodiments, the organic solvent comprises THF.

The organic solvent may be present in an amount of 10 L/kg of Compound L to 25 L/kg of Compound L, such as a minimum of 10, 15, 20 L/kg of Compound L, and/or a maximum of 25, 20, or It may be present in an amount of 15 L/kg of Compound L, such as 10-20 L/kg of Compound L, 10-15 L/kg of Compound L, or 15 L/kg to 22 L/kg of Compound L. .

In some embodiments, the compound L can be slowly added to the mixture containing Ar ¹ -SH and the non-nucleophilic base. In some embodiments, Compound L is added dropwise to a mixture comprising Ar ¹ -SH and a non-nucleophilic base over 3 hours to 6 hours, such as 3 hours, 3.5 hours, 4 hours, 5 hours. , 5.5 hours, or 6 hours. In some embodiments, Compound L is added dropwise to a mixture containing Ar ¹ -SH and a non-nucleophilic base over 5 hours.

In some embodiments, the mixing of step (e) is conducted for 3 to 5 hours, such as 3 hours, 3.5 hours, 4 hours, 4.5 hours, or 5 hours. In some embodiments, the mixing of step (e) is performed for 4 hours.

The mixing of step (e) may be carried out at a temperature of 60° C. to 80° C., such as at a temperature as low as 60 or 65° C., and/or at a temperature as high as 80, 75, 70, or 68, such as , 60°C to 75°C, 65°C to 75°C, or 65°C to 80°C. In some embodiments, this mixing is performed at a temperature of 68°C.

The formation of compound M in step (e) can be processed directly to the next step without the need for substantial purification. In some embodiments, compound M is washed 3-5 times with aqueous sodium hydroxide prior to oxidation in step (f). Advantageously, washing compound M 3-5 times (eg 5 times) removes residual Ar ¹ -SH, resulting in improved purity profiles and yields as well as further purification (eg chromatographic purification) are avoided.

の構造を有しており、式中、Ａｒ^１は、上記で定義された通りである。 Oxidation of compound M to form compound N (step (f))
The methods of the present disclosure involve oxidation of compound M to give compound N. This oxidation involves combining compound M and an oxidizing agent to form compound N. As provided herein, compound N is

where Ar ¹ is as defined above.

Suitable oxidizing agents are well known in the art. Non-limiting examples of oxidizing agents include: peracids, such as m-chloroperbenzoic acid (mCPBA), hydrogen peroxide, tert-butyl hydroperoxide, and the like; perchloric acid, such as , tetrabutylammonium perchlorate and the like; chlorates such as sodium chlorate and the like; chlorites such as sodium chlorite and the like; hypochlorite , such as bleach and the like, periodates such as sodium periodate and the like; highly valent iodine reagents such as iodosylbenzene, iodobenzene diacetate, and the like; manganese; reagents containing such as manganese dioxide, potassium permanganate, and the like; lead, such as lead tetraacetate and the like; reagents containing chromium, such as pyridinium chlorochromate (PCC), pyridinium dichromate (PDC), Jones reagent, and the like; halogen compounds such as N-bromosuccinimide (NBS) and the like; oxygen; ozone; sulfur trioxide-pyridine complex; 6-dicyano-1,4-benzoquinone (DDQ). In some embodiments, the oxidizing agent is hydrogen peroxide.

Compound M and oxidizing agent may be present in a molar ratio of 1:1.3 to 1:5, such as a minimum of 1:1.3, 1:1.5, 1:2, or 1:3, and /or may be present in molar ratios up to 1:3, 1:2, 1:1.8, or 1:1.5, such as from 1:1.3 to 1:4, from 1:1.3 to It can be present in a molar ratio of 1:3, 1:1.3 to 1:2, or 1:1.3 to 1:1.8. In some embodiments, the molar ratio of compound M to oxidizing agent is 1:1.5.

Oxidizing compound M may further comprise combining compound M and an oxidizing agent with an oxidation catalyst. Non-limiting examples of oxidation catalysts include: 2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl (TEMPO), tetrapropylammonium perruthenate (TPAP), 9-azabicyclo [ 3.3.1] nonane N-oxyl (ABNO), metal catalyst (e.g. copper, iron, etc.), 2-azaadamantane-N-oxyl, 1-methyl-2-azaadamantane-N-oxyl, 1,3 -dimethyl-2-azaadamantane-N-oxyl, 4-acetamido-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate, sodium tungstate dehydrate, and 3 - chloroperbenzoic acid. In some embodiments, the oxidation catalyst is sodium tungstate dehydrate, 3-chloroperbenzoic acid, or a combination thereof. In some embodiments, the oxidation catalyst is sodium tungstate dehydrate. In some embodiments, the mixing of step (f) can include hydrogen peroxide and sodium tungstate dehydrate.

When an oxidation catalyst is present, compound M and oxidation catalyst may be present in a molar ratio of 1:0.05 to 1:0.5, such as a minimum of 1:0.05, 0.04, 1 : 0.1, 1:0.2, 1:0.3, or 1:0.5 and/or up to 1:0.5, 1:0.4, 1:0.3, 1:0 .2, or 1:0.1 molar ratio, for example from 1:0.05 to 1:0.4, from 1:0.05 to 1:0.3, or from 1:0.05 May be present in a molar ratio of 1:0.2. In some embodiments, the molar ratio of compound M to oxidation catalyst is 1:0.1.

In some embodiments, the oxidizing of step (f) further comprises acetic acid. Advantageously, when mixed with acetic acid during the oxidation step, the acetic acid may enhance safety by allowing a reduction in the amount of hydrogen peroxide used, and the purity profile of Compound N is can be improved and conversion to product can be increased since the acetic acid stabilizes the hydrogen peroxide reagent.

In some embodiments, the oxidation of step (f), which is an oxidation reaction, can be performed in a solvent such as an alcoholic solvent (eg, methanol, ethanol, isopropanol). In some embodiments, the solvent is methanol.

In some embodiments, the oxidizing of step (f) is performed for 12 hours to 48 hours, such as 12 hours, 15 hours, 20 hours, 24 hours, 30 hours, 35 hours, 40 hours, or 48 hours. Do it over time. In some embodiments, the mixing of step (f) is performed for 24 hours.

In some embodiments, the oxidizing of step (f) can be performed at a temperature maintained at 25°C ± 5°C. In some embodiments, the oxidizing of step (f) is performed at a temperature of 20°C to 25°C.

In some embodiments, compound N may crystallize from the oxidation of step (f). In some embodiments, crystallization of compound N may be performed by adding water to the oxidation of step (f). Advantageously, the crystallization of compound N is carried out by the addition of water to the oxidation of step (f), where direct crystallization prior to extraction of compound N not only improves throughput and yield. , the purity profile of the reaction mixture is improved.

の構造を有する。 Sulfonamidation of Compound N to Form Compound Z The method of the present disclosure involves compound N sulfonamidation to obtain compound Z (step (g)). The sulfonamidation involves combining compound N, a base, and hydroxylamine-O-sulfonic acid to form compound Z. As provided herein, compound Z is

has the structure

の構造を有しており、式中、Ｑは、アルカリ金属カチオンである。一部の実施形態では、Ｑは、リチウム、ナトリウム、カリウム、又はこれらの組合せである。一部の実施形態では、Ｑは、ナトリウムである。一部の実施形態では、化合物Ｎ及び塩基の混合を、溶媒中で行なう。一部の実施形態では、この溶媒は、ｔｅｒｔ－ブチルメチルエーテル、メタノール、テトラヒドロフラン、２－メチルテトラヒドロフラン、又はこれらの組合せを含む。一部の実施形態では、この溶媒は、ｔｅｒｔ－ブチルメチルエーテル及びメタノールを含む。 In some embodiments, compound N and a base are mixed together in a solvent to form intermediate compound O, which is then mixed with hydroxylamino-O-sulfonic acid. As provided herein, compound O is

where Q is an alkali metal cation. In some embodiments, Q is lithium, sodium, potassium, or combinations thereof. In some embodiments, Q is sodium. In some embodiments, the mixing of Compound N and the base is performed in a solvent. In some embodiments, the solvent comprises tert-butyl methyl ether, methanol, tetrahydrofuran, 2-methyltetrahydrofuran, or combinations thereof. In some embodiments, the solvent comprises tert-butyl methyl ether and methanol.

In some embodiments, the base comprises sodium thiomethoxide, sodium methoxide, potassium carbonate and methanol, or combinations thereof. In some embodiments, the base comprises sodium thiomethoxide.

In some embodiments, compound N and the base are mixed for 6 hours to 18 hours, such as 6 hours, 8 hours, 10 hours, 12 hours, 14 hours, 15 hours, or 18 hours. In some embodiments, the mixing of Compound N and the base is performed for 12 hours.

In some embodiments, the mixing of Compound N and the base can be performed at a temperature of 25° C. to 50° C., for example, a minimum of 25, 30, 35, 40° C., and/or a maximum of 50, 45, 40, or at a temperature of 35°C, for example at a temperature of 25°C to 45°C, 30°C to 45°C, or 30°C to 40°C. In some embodiments, the mixing of Compound N and the base is performed at a temperature of 35°C.

In some embodiments, mixing compound N and a base provides intermediate compound O, which can be processed directly into the addition of hydroxylamine-O-sulfonic acid without the need for substantial purification. In some embodiments, hydroxylamine-O-sulfonic acid is added to this intermediate compound O along with sodium acetate, potassium acetate, sodium formate, potassium formate, or combinations thereof. In some embodiments, to this intermediate compound O is added hydroxylamine-O-sulfonic acid along with sodium acetate. In some embodiments, to this intermediate compound O is added hydroxylamine-O-sulfonic acid along with sodium acetate trihydrate.

In some embodiments, mixing intermediate compound O, hydroxylamine-O-sulfonic acid, and sodium acetate is performed in a solvent. In some embodiments, the solvent comprises tert-butyl methyl ether, methanol, 2-methyltetrahydrofuran, or combinations thereof. In some embodiments, the solvent comprises tert-butyl methyl ether and methanol. In some embodiments, the solvent can be a biphasic mixture. In some embodiments, this biphasic mixture comprises water and an organic solvent such as tert-butyl methyl ether.

In some embodiments, the mixture of intermediate compound O, hydroxylamine-O-sulfonic acid, and sodium acetate is run for 30 minutes to 4 hours, for example, 30 minutes 1 hour, 1.5 hours, 2 hours, Run for 2.5 hours, 3 hours, 3.5 hours, or 4 hours. In some embodiments, the mixing of intermediate compound O, hydroxylamine-O-sulfonic acid, and sodium acetate is performed for 2 hours.

In some embodiments, the mixing of intermediate compound O, hydroxylamine-O-sulfonic acid, and sodium acetate can be carried out at a temperature of 25°C to 50°C, such as a minimum of 25, 30, 35, 40°C. , and/or up to 50, 45, 40, or 35°C, such as 25°C to 45°C, 30°C to 45°C, or 30°C to 40°C. In some embodiments, mixing intermediate compound O, hydroxylamine-O-sulfonic acid, and sodium acetate is performed at a temperature of 35°C.

In some embodiments, compound Z may be crystallized from the sulfonamidation of step (g). In some embodiments, crystallization of compound Z is accomplished by heating a solution of compound Z, then cooling the solution and adding a crystallization solvent to the cooled solution to form crystals of compound Z. Including. In some embodiments, the crystallizing comprises heating a solution of compound Z to 40° C.-45° C., then cooling the solution to 10° C.-15° C., and crystallizing into the cooled solution. A solvent is added to form compound Z crystals. In some embodiments, the solution of compound Z comprises tert-butyl methyl ether and the crystallization solvent comprises heptane. In some embodiments, the solution of compound Z comprises methanol and the crystallization solvent comprises water. Advantageously, crystallization of compound Z comprises heating a solution of compound Z to 40° C.-45° C., which prevents melting of compound Z, controls crystallization and increases yield. and improved purity profile. In addition, crystallization of compound Z involves heating a solution of compound Z to 40° C.-45° C., which increases product purity, removes chiral impurities, and induces crystallization of alternative chiral impurities. Rejected. Crystallization of compound Z advantageously purifies the product without chromatography and its attendant loss of yield.

Compounds A1 and A2 can be synthesized using compound Z prepared by the methods disclosed herein. As shown in Scheme 3, compound Z can be used to synthesize compound A1 and its salts and solvates, and as shown in scheme 4, compound Z can be used to synthesize compound A2 and its salts and solvates. You can synthesize things.

スキーム３に示すように、且つ米国特許第９，５６２，０６１号明細書で説明されているように、化合物Ｚを使用して、化合物Ａ１並びにその塩及び溶媒和物を合成し得る。ＡＡ１１Ａの合成は、米国特許第９，５６２，０６１号明細書で開示されている。米国特許第９，５６２，０６１号明細書に記載されているように、化合物Ｚ及びＡＡ１１Ａを反応させて、化合物Ｂを形成し得る。化合物Ｂの環化により、ヒドロキシ化合物Ｃが得られ、次いで、このヒドロキシ化合物Ｃをメチル化させることにより、米国特許第９，５６２，０６１号明細書で説明されている化合物Ａ１が得られる。 Scheme 3 - Conversion of Compound Z to Compound A1

Compound Z can be used to synthesize compound A1 and its salts and solvates as shown in Scheme 3 and as described in US Pat. No. 9,562,061. The synthesis of AA11A is disclosed in US Pat. No. 9,562,061. Compound Z and AA11A can be reacted to form compound B as described in US Pat. No. 9,562,061. Cyclization of compound B gives hydroxy compound C, which is then methylated to give compound A1 as described in US Pat. No. 9,562,061.

スキーム４に示すように、且つ米国特許第１０，３００，０７５号明細書で説明されているように、化合物Ｚを使用して、化合物Ａ２並びにその塩及び溶媒和物を合成し得る。スキーム３に関して上記で説明されているように、ＡＡ１１Ａの合成は、米国特許第９，５６２，０６１号明細書で開示されている。上記で説明されているように、且つ米国特許第９，５６２，０６１号明細書に記載されているように、スルホンアミドＺ及びＡＡ１１Ａを反応させて化合物Ｂを形成し得、この化合物Ｂを環化させてヒドロキシ化合物Ｃを生成し得る。次いで、化合物Ｃを酸化させて、米国特許第１０，３００，０７５号明細書で開示されている環状エノンＤを得ることができる。或いは、化合物Ｂを酸化させて化合物Ｃの非環化エノンバージョンを生成し、次いで環化させて環状エノンＤを得ることができる。次いで、エノンＤを、米国特許第１０，３００，０７５号明細書で開示されている手順を使用してエポキシドＥに変換させ得る。次いで、エポキシドＥを、二環式化合物Ｆと反応させて、ヒドロキシ化合物Ｇを得ることができる。最後に、化合物Ｇのメチル化により、米国特許第１０，３００，０７５号明細書で開示されているように化合物Ａ２が得られる。 Scheme 4 - Conversion of Compound Z to Compound A2

Compound Z can be used to synthesize compound A2 and its salts and solvates as shown in Scheme 4 and as described in US Pat. No. 10,300,075. As explained above with respect to Scheme 3, the synthesis of AA11A is disclosed in US Pat. No. 9,562,061. As explained above and as described in US Pat. No. 9,562,061, sulfonamide Z and AA11A can be reacted to form compound B, which is converted into a ring to form hydroxy compound C. Compound C can then be oxidized to give the cyclic enone D disclosed in US Pat. No. 10,300,075. Alternatively, compound B can be oxidized to produce the uncyclized enone version of compound C, followed by cyclization to give the cyclic enone D. Enone D can then be converted to epoxide E using the procedures disclosed in US Pat. No. 10,300,075. Epoxide E can then be reacted with bicyclic compound F to give hydroxy compound G. Finally, methylation of compound G gives compound A2 as disclosed in US Pat. No. 10,300,075.

While the present disclosure should be read in conjunction with the detailed description thereof, the foregoing description and the following examples are illustrative and do not limit the scope of the present disclosure, which is defined by the appended claims. It should be understood that the ranges are intended to be defined. Other aspects, advantages, and modifications are within the scope of the following claims.

The following examples are provided for illustration and are not intended to limit the scope of the invention.

Example 1: Formation of Compound Z

（２Ｓ，３Ｒ）－３－ブロモブタン－２－イル アセテート（化合物Ｉ）：２０Ｌのガラス裏地のジャケット付き反応器に、臭化水素（酢酸中の３３ｗ／ｗ％溶液、３．５ｋｇ、１４．３ｍｏｌ、３．５当量）を充填した。この溶液を＋１０℃まで冷却し、温度を＋１０℃以下（ＮＭＴ＋１０℃）に維持しつつ、（２Ｓ，３Ｓ）－ブタン－２，３－ジオール（３６８ｇ、４．０８ｍｏｌ、１．０当量）を緩やかに添加した。この混合物を、１５～２０時間にわたり＋１０℃で撹拌した。次いで、温度を＋１０℃未満に維持しつつ、この反応混合物を、水（３．６８Ｌ、１０．０Ｌ／ｋｇ）中の炭酸カリウム（１．８４ｋｇ、３．２６当量）の予め冷却した撹拌溶液に、８時間かけて緩やかに添加した。この混合物を、ｔｅｒｔ－ブチルメチルエーテル（１．８４Ｌ、５．００Ｌ／ｋｇ）で希釈し、＋２０～＋２５℃まで温め、少なくとも３０分間撹拌した。相を分離し、得られた水層を、ｔｅｒｔ－ブチルメチルエーテル（１．１０Ｌ、３．００Ｌ／ｋｇ）で洗浄した。まとめた有機層を、炭酸カリウム（６４４ｇ、１．１４当量）の水（２．４Ｌ、６．５Ｌ／ｋｇ）溶液で洗浄した。有機層を、水（７４０ｍＬ、２．０Ｌ／ｋｇ）で洗浄し、＋４５℃で減圧下にて希釈した。蒸留の終了時に、この溶液をサンプリングして低い含水量を確認し、ｔｅｒｔ－ブチルメチルエーテルで約１．１０Ｌの全量（３Ｌ／ｋｇ）まで希釈した。効力調整アッセイ（ｐｏｔｅｎｃｙ－ａｄｊｕｓｔｅｄ ａｓｓａｙ）収率は、９５～９７％であり、典型的なＧＣ純度は、９５．０Ａｒｅａ％超であった。ｔｅｒｔ－メチルメチルエーテル中の化合物Ｉの得られた溶液は、このプロセスの次の工程での直接的な使用に好適であった。 Synthesis of Compound I

(2S,3R)-3-bromobutan-2-yl acetate (Compound I): Hydrogen bromide (33 w/w % solution in acetic acid, 3.5 kg, 14.3 mol) was added to a 20 L glass-lined jacketed reactor. , 3.5 equivalents) were charged. The solution was cooled to +10° C. and (2S,3S)-butane-2,3-diol (368 g, 4.08 mol, 1.0 eq) was slowly added while maintaining the temperature below +10° C. (NMT+10° C.). was added to The mixture was stirred at +10° C. for 15-20 hours. The reaction mixture was then transferred to a pre-cooled stirred solution of potassium carbonate (1.84 kg, 3.26 eq) in water (3.68 L, 10.0 L/kg) while maintaining the temperature below +10°C. was slowly added over 8 hours. The mixture was diluted with tert-butyl methyl ether (1.84 L, 5.00 L/kg), warmed to +20-+25° C. and stirred for at least 30 minutes. The phases were separated and the resulting aqueous layer was washed with tert-butyl methyl ether (1.10 L, 3.00 L/kg). The combined organic layers were washed with a solution of potassium carbonate (644 g, 1.14 eq) in water (2.4 L, 6.5 L/kg). The organic layer was washed with water (740 mL, 2.0 L/kg) and diluted under reduced pressure at +45°C. At the end of distillation, the solution was sampled for low water content and diluted with tert-butyl methyl ether to a total volume of approximately 1.10 L (3 L/kg). Potency-adjusted assay yields were 95-97% with typical GC purities greater than 95.0 Area%. The resulting solution of compound I in tert-methyl methyl ether was suitable for direct use in the next step of the process.

A sample of Compound I was concentrated in vacuo for characterization by NMR. ¹ H NMR (300 MHz, CDCl ₃ ) δ 4.84-4.78 (m, 1H), 4.16-4.04 (m, 1H), 1.96 (s, 3H), 1.55 (d , J=7.1 Hz, 3H), 1.21 (d, J=6.9 Hz, 3H). LRMS _{( ESI} ): calcd for _C6H11Br1O2 + _Na : 217.0, found: 217.0.

（２Ｓ，３Ｓ）－２，３－ジメチルオキシラン（化合物Ｊ）：２０Ｌのガラス裏地のジャケット付き反応器に、モノエチレングリコール（１．２２Ｌ、２．８８Ｌ／ｋｇ）を充填した。温度を＋４０℃未満に維持しつつ、固体のカリウム ｔｅｒｔ－ブトキシド（６１２ｇ、５．４５ｍｏｌ、２．５０当量）を、約５時間かけて少量ずつ添加した。得られた混合物を、＋９０～１２０℃で減圧下にて蒸留し、ｔｅｒｔ－ブタノール 約５００ｍＬを除去した。溶媒であるｔｅｒｔ－ブチルメチルエーテル（２．１３Ｌ、５．０Ｌ／ｋｇ）を添加し、この混合物を、ｔｅｒｔ－ブタノール含有量がＧＣにより０．４ｗｔ／ｗｔ％未満と測定されるまで、減圧下で蒸留した。＋３０℃まで冷却した後、化合物Ｉ（４２５ｇ、２．１８ｍｏｌ、１．０当量）のｔｅｒｔ－ブチルメチルエーテル（４２５ｍＬ、１．００Ｌ／ｋｇ）溶液を、３０分かけて添加し、その後、裏地をｔｅｒｔ－ブチルメチルエーテル（４２５ｍＬ、１．００Ｌ／ｋｇ）で洗浄した。得られた混合物を、＋３０℃で３０分にわたり撹拌した。この反応混合物を、減圧下でそのまま蒸留した（コンデンサーの設定－１５℃）。生成物である化合物Ｊが、７５～８０％の効力調整収率（ｐｏｔｅｎｃｙ－ａｄｊｕｓｔｅｄ ｙｉｅｌｄ）で得られ、典型的なＧＣ純度は、９８．０Ａｒｅａ％超であった。得られたＳＳ－ＤＭＯの溶液（ｔｅｒｔ－ブチルメチルエーテルが残留している）は、このプロセスの次の工程でのそのままでの使用に好適であった。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＣＤＣｌ_３）δ ２．６４－２．５８（ｍ，２Ｈ），１．１９－１．１５（ｍ，６Ｈ）． Synthesis of compound J

(2S,3S)-2,3-Dimethyloxirane (Compound J): A 20 L glass lined jacketed reactor was charged with monoethylene glycol (1.22 L, 2.88 L/kg). Solid potassium tert-butoxide (612 g, 5.45 mol, 2.50 eq) was added in portions over about 5 hours while maintaining the temperature below +40°C. The resulting mixture was distilled under reduced pressure at +90-120° C. to remove approximately 500 mL of tert-butanol. The solvent tert-butyl methyl ether (2.13 L, 5.0 L/kg) was added and the mixture was evacuated under reduced pressure until the tert-butanol content was determined by GC to be less than 0.4 wt/wt%. distilled at After cooling to +30° C., a solution of compound I (425 g, 2.18 mol, 1.0 eq.) in tert-butyl methyl ether (425 mL, 1.00 L/kg) was added over 30 minutes, after which the liner was Washed with tert-butyl methyl ether (425 mL, 1.00 L/kg). The resulting mixture was stirred at +30° C. for 30 minutes. The reaction mixture was distilled neat under reduced pressure (condenser setting -15°C). The product, Compound J, was obtained in a potency-adjusted yield of 75-80% with a typical GC purity of >98.0 Area%. The resulting solution of SS-DMO (remaining tert-butyl methyl ether) was suitable for use as such in the next step of the process.
¹ H NMR (300 MHz, CDCl ₃ ) δ 2.64-2.58 (m, 2H), 1.19-1.15 (m, 6H).

（２Ｓ，３Ｓ）－３－メチルヘキサ－５－エン－２－オール（化合物Ｋ）：２０Ｌのガラス裏地のジャケット付き反応器に、アリルマグネシウムクロリドのテトラヒドロフラン溶液（１８ｗ／ｗ％溶液、７．２８ｍｏｌ、１．２０当量）を充填し、＋７～＋１０℃まで冷却した。温度を＋７℃未満に維持しつつ、化合物Ｊ（４３８ｇ、６．０７ｍｏｌ、１．００当量）のｔｅｒｔ－ブチルメチルエーテル（６５７ｍＬ、１．５Ｌ／ｋｇ）溶液を、３時間かけて滴下した。この反応物を、さらに３時間にわたり＋７～＋１０℃で撹拌した。温度を＋５～＋１０℃に維持しつつ、この反応混合物を、水（３．５０Ｌ、８．００Ｌ／ｋｇ）中のクエン酸一水和物（１．６８ｋｇ、７．８９ｍｏｌ、１．３当量）の予め冷却した撹拌溶液に、２～３時間かけて滴下した。得られた混合物を、＋２５℃まで温め、３０分にわたり撹拌した。相を分離し、水層をｔｅｒｔ－ブチルメチルエーテルで２回洗浄した（２×８７６ｍＬ、２×２．００Ｌ／ｋｇ）。有機層をまとめ、炭酸水素ナトリウム水溶液で２回洗浄し（０．８ｍｏｌ／Ｌ溶液；２×２．６３Ｌ、２×６．０Ｌ／ｋｇ）、次いで塩化ナトリウム水溶液で２回洗浄した（５．３ｍｏｌ／Ｌ溶液；２×８７６ｍＬ、２×２．０Ｌ／ｋｇ）。この有機層を、＋３０℃で減圧下にて、総量１．３Ｌ（３．０Ｌ／ｋｇ）まで蒸留した。溶媒であるテトラヒドロフランを３回添加し（３×１．３Ｌ、３×３．０Ｌ／ｋｇ）、この混合物を、＋３０℃で減圧下にて、最終量１．３Ｌ（３．０ｋｇ）まで蒸留した。効力調整アッセイ収率は、９０～９５％であり、典型的なＧＣ純度は、８８．０Ａｒｅａ％超であった。得られた化合物Ｋのテトラヒドロフラン溶液は、このプロセスの次の工程でのそのままでの使用に好適であった。 Synthesis of Compound K

(2S,3S)-3-Methylhex-5-en-2-ol (Compound K): In a 20 L glass-lined jacketed reactor, allylmagnesium chloride in tetrahydrofuran (18 w/w % solution, 7.28 mol, 1.20 eq) and cooled to +7-+10°C. A solution of compound J (438 g, 6.07 mol, 1.00 eq) in tert-butyl methyl ether (657 mL, 1.5 L/kg) was added dropwise over 3 hours while maintaining the temperature below +7°C. The reaction was stirred at +7-+10° C. for an additional 3 hours. The reaction mixture was treated with citric acid monohydrate (1.68 kg, 7.89 mol, 1.3 eq) in water (3.50 L, 8.00 L/kg) while maintaining the temperature between +5 and +10°C. was added dropwise over a period of 2-3 hours to a pre-cooled stirred solution of . The resulting mixture was warmed to +25° C. and stirred for 30 minutes. The phases were separated and the aqueous layer was washed twice with tert-butyl methyl ether (2 x 876 mL, 2 x 2.00 L/kg). The organic layers were combined and washed twice with aqueous sodium bicarbonate (0.8 mol/L solution; 2 x 2.63 L, 2 x 6.0 L/kg) and then twice with aqueous sodium chloride (5.3 mol /L solution; 2 x 876 mL, 2 x 2.0 L/kg). The organic layer was distilled at +30° C. under reduced pressure to a total volume of 1.3 L (3.0 L/kg). The solvent tetrahydrofuran was added three times (3 x 1.3 L, 3 x 3.0 L/kg) and the mixture was distilled under reduced pressure at +30°C to a final volume of 1.3 L (3.0 kg). . Potency-adjusted assay yields were 90-95% with typical GC purities >88.0 Area%. The resulting tetrahydrofuran solution of compound K was suitable for use as such in the next step of the process.

A sample of Compound K was concentrated in vacuo for characterization by NMR. ¹ H NMR (300 MHz, CDCl ₃ ) δ 5.81-5.67 (m, 1H), 5.02-4.89 (m, 2H), 3.70-3.63 (m, 1H), 2 .22-2.10 (m, 1H), 1.90-1.75 (m, 2H), 1.15 (d, J=7.0Hz, 3H), 0.82 (d, J=6. 9Hz, 3H). LRMS ( _ESI ): calc'd for _C7H14O1 +Na: 137.1, found _: 137.1.

（２Ｓ，３Ｓ）－３－メチルヘキサ－５－エン－２－イル メタンスルホネート（化合物Ｌ、式中、ＬＧは、ＯＭｓであった）：２０Ｌのガラス裏地のジャケット付き反応器に、化合物Ｋ（７１７ｇ、４．９７ｍｏｌ、１．００当量）のテトラヒドロフラン（７００ｍＬ、１．０Ｌ／ｋｇ）溶液、及び溶媒であるｔｅｒｔ－ブチルメチルエーテル（５．７Ｌ、８．０Ｌ／ｋｇ）を充填した。この混合物を、０℃まで冷却し、トリエチルアミン（２．０１Ｌ、１１．４ｍｏｌ、２．３０当量）を充填し、続いてｔｅｒｔ－ブチルメチルエーテル（７００ｍＬ、１Ｌ／ｋｇ）を充填した。０～＋５℃で、メタンスルホニルクロリド（６８０ｍＬ、６．９６ｍｏｌ、１．４０当量）を、２．５時間かけて緩やかに添加した。この反応物を、３０分にわたり＋５℃で撹拌した。次いで、１５℃未満で、塩酸水溶液（１ｍｏｌ／Ｌ溶液；５．０Ｌ、７．０Ｌ／ｋｇ、１．０当量）を、３０分かけて添加した。この二相混合物を、＋２５℃まで温め、６時間撹拌し、次いで相を分離した。水層を、ｔｅｒｔ－ブチルメチルエーテル（２．９Ｌ、４．０Ｌ／ｋｇ）で抽出した。まとめた有機相を、塩酸水溶液（１ｍｏｌ／Ｌ溶液；２．９Ｌ、４．０Ｌ／ｋｇ、０．６当量）で洗浄し、塩化ナトリウム水溶液で２回洗浄し（５．７ｍｏｌ／Ｌ溶液；２×１．４Ｌ、２×３．０Ｌ／ｋｇ）、水で洗浄した（１．４Ｌ、２．０Ｌ／ｋｇ）。この有機相を、減圧下で、総量２．９Ｌ（４．０Ｌ／ｋｇ）まで蒸留した。テトラヒドロフラン（２．９Ｌ、４．０Ｌ／ｋｇ）を添加し、この混合物を、減圧下で、総量２．９Ｌ（４．０Ｌ／ｋｇ）まで再度蒸留した。効力調整アッセイ収率は、９３～９７％であり、典型的なＧＣ純度は、９８．０Ａｒｅ％超であった。得られた化合物Ｌ（式中、ＬＧは、ＯＭｓである）のテトラヒドロフラン溶液は、このプロセスの次の工程でのそのままでの使用に好適であった。 Synthesis of compound L (where LG is OMs)

(2S,3S)-3-Methylhex-5-en-2-yl methanesulfonate (Compound L, where LG was OMs): Compound K (717 g) was added to a 20 L glass-lined jacketed reactor. , 4.97 mol, 1.00 eq.) in tetrahydrofuran (700 mL, 1.0 L/kg) and solvent tert-butyl methyl ether (5.7 L, 8.0 L/kg) were charged. The mixture was cooled to 0° C. and charged with triethylamine (2.01 L, 11.4 mol, 2.30 eq) followed by tert-butyl methyl ether (700 mL, 1 L/kg). At 0-+5° C., methanesulfonyl chloride (680 mL, 6.96 mol, 1.40 eq) was added slowly over 2.5 hours. The reaction was stirred at +5° C. for 30 minutes. Then, below 15° C., aqueous hydrochloric acid (1 mol/L solution; 5.0 L, 7.0 L/kg, 1.0 equivalent) was added over 30 minutes. The biphasic mixture was warmed to +25° C. and stirred for 6 hours, then the phases were separated. The aqueous layer was extracted with tert-butyl methyl ether (2.9L, 4.0L/kg). The combined organic phases were washed with aqueous hydrochloric acid (1 mol/L solution; 2.9 L, 4.0 L/kg, 0.6 eq) and twice with aqueous sodium chloride (5.7 mol/L solution; 2 × 1.4 L, 2 × 3.0 L/kg), washed with water (1.4 L, 2.0 L/kg). The organic phase was distilled under reduced pressure to a total volume of 2.9 L (4.0 L/kg). Tetrahydrofuran (2.9 L, 4.0 L/kg) was added and the mixture was distilled again under reduced pressure to a total volume of 2.9 L (4.0 L/kg). Potency-adjusted assay yields were 93-97% with typical GC purities greater than 98.0 Are%. The resulting tetrahydrofuran solution of compound L (where LG is OMs) was suitable for use as such in the next step of the process.

２－（（（２Ｒ，３Ｓ）－３－メチルヘキサ－５－エン－２－イル）チオ）ピリジン（化合物Ｍ、式中、Ａｒ^１は、ピリジニルである）：２０Ｌのガラス裏地のジャケット付き反応器に、２－チオピリジン（６３７ｇ、５．７３ｍｏｌ、１．０８当量）及びテトラヒドロフラン（１０．０Ｌ、９．０Ｌ／ｋｇ）を充填し、得られた混合物を、１５℃で３０分にわたり撹拌した。温度をＮＭＴ＋３０℃に維持しつつ、ナトリウム ｔｅｒｔｐ－ブトキシド（６１２ｇ、６．３７ｍｏｌ、１．２０当量）を、１時間かけて少量ずつ添加した。添加後、この反応混合物を加熱して、１時間かけて＋６８℃で緩やかに還流させた。この温度で、化合物Ｌ（式中、ＬＧは、ＯＭｓである）（１，０２０ｇ、５．３１ｍｏｌ、１．００当量）のテトラヒドロフラン（１．０Ｌ、１．０Ｌ／ｋｇ）溶液を、５時間かけて滴下した。この反応物を、さらに４時間にわたり撹拌した。この反応混合物を、＋６５～＋７５℃で大気圧にて蒸留して、溶媒 約６Ｌを除去した。この混合物を、＋２０℃まで冷却し、水（３．０Ｌ、３．０Ｌ／ｋｇ）及び酢酸エチル（５．０Ｌ、５．０Ｌ／ｋｇ）を添加した。この混合物を、固体が全体として溶解するまで、＋２５℃で３０分にわたり撹拌した。層を分離し、水層を酢酸エチル（３．０Ｌ、３．０Ｌ／ｋｇ）で抽出した。まとめた有機相を、水酸化ナトリウム水溶液で５回洗浄し（１ｍｏｌ／Ｌ溶液；５×２．２Ｌ、５×２．２Ｌ／ｋｇ）、次いで水で１回洗浄した（４．０Ｌ、４．０Ｌ／ｋｇ）。この有機層を、総量３Ｌまで真空蒸留した。メタノールを２回添加し（２×５．０Ｌ、２×５．０Ｌ／ｋｇ）、この混合物を、総量３Ｌまで蒸留した。抗力調整アッセイ収率は、６８～７５％であり、典型的なＬＣ純度は、９５．０Ａｒｅａ％超であった。得られた化合物Ｍ（式中、Ａｒ^１は、ピリジニルである）のメタノール溶液は、このプロセスの次の工程でのそのままでの使用に好適であった。 Synthesis of compound M, where Ar ¹ is pyridinyl

2-(((2R,3S)-3-methylhex-5-en-2-yl)thio)pyridine (compound M, where Ar ¹ is pyridinyl): 20 L glass lined jacketed reactor was charged with 2-thiopyridine (637 g, 5.73 mol, 1.08 eq) and tetrahydrofuran (10.0 L, 9.0 L/kg) and the resulting mixture was stirred at 15° C. for 30 minutes. Sodium tertp-butoxide (612 g, 6.37 mol, 1.20 eq) was added in portions over 1 hour while maintaining the temperature at NMT +30°C. After the addition, the reaction mixture was heated to gentle reflux at +68° C. for 1 hour. At this temperature, a solution of compound L (wherein LG is OMs) (1,020 g, 5.31 mol, 1.00 eq) in tetrahydrofuran (1.0 L, 1.0 L/kg) was added over 5 hours. dripped. The reaction was stirred for an additional 4 hours. The reaction mixture was distilled at +65 to +75° C. at atmospheric pressure to remove approximately 6 L of solvent. The mixture was cooled to +20° C. and water (3.0 L, 3.0 L/kg) and ethyl acetate (5.0 L, 5.0 L/kg) were added. The mixture was stirred at +25° C. for 30 minutes until all solids dissolved. The layers were separated and the aqueous layer was extracted with ethyl acetate (3.0L, 3.0L/kg). The combined organic phases were washed five times with aqueous sodium hydroxide (1 mol/L solution; 5 x 2.2 L, 5 x 2.2 L/kg) and then once with water (4.0 L, 4.0 L/kg). 0 L/kg). The organic layer was vacuum distilled to a total volume of 3L. Methanol was added twice (2 x 5.0 L, 2 x 5.0 L/kg) and the mixture distilled to a total volume of 3 L. Drag-adjusted assay yields were 68-75% and typical LC purities were greater than 95.0 Area%. The resulting methanolic solution of compound M (wherein Ar ¹ is pyridinyl) was suitable for use as such in the next step of the process.

A sample of compound M (where Ar ¹ is pyridinyl) was concentrated in vacuo for characterization by NMR. ¹ H NMR (300 MHz, CDCl ₃ ) δ 8.30 (dd, J=1.2, 5.1 Hz, 1 H), 7.36 (ddd, J=1.2, 7.9, 8.2 Hz, 1 H ), 7.08 (d, J=7.9 Hz, 1 H), 6.85 (dd, J=5.1, 8.2 Hz, 1 H). LRMS ( _ESI ): calcd for _C12H17N1S1 +Na: _230.1 , found: _230.1 .

２－（（（２Ｒ，３Ｓ）－３－メチルヘキサ－５－エン－２－イル）スルホニル）ピリジン（化合物Ｎ、式中、Ａｒ^１は、ピリジニルである）：１０Ｌのガラス裏地のジャケット付き反応器に、化合物Ｍ（式中、Ａｒ^１は、ピリジニルである）（４６８ｇ、２．２６ｍｏｌ、１．００当量）を充填し、この混合物を、メタノールで（１．４Ｌ、３．０Ｌ／ｋｇ）で希釈した。酢酸（１３６ｇ、２．２６ｍｏｌ、１．００当量）を添加し、次いで、タングステン酸ナトリウム脱水和物（７５ｇ、０．２３ｍｏｌ、０．１０当量）を添加した。この混合物を＋２５℃で撹拌し、温度をＮＭＴ＋２５℃に維持しつつ、過酸化水素（２７６ｇ、２．９４ｍｏｌ、１．３当量）を４．５時間かけて添加した。この添加が完了した後、この反応物を２４時間にわたり撹拌した。水（２．３４Ｌ、５．０Ｌ／ｋｇ）を１時間かけて添加して、結晶化を誘発した。この結晶化混合物を、０℃まで冷却し、２時間にわたり撹拌した。次いで、この生成物を、０℃でろ別し、次いで、湿ったケーキを、＋２５℃で、チオ硫酸ナトリウム水溶液（１．２ｍｏｌ／Ｌ溶液；１．８７Ｌ、４．０Ｌ／ｋｇ、２．２６ｍｏｌ、１．００当量）との撹拌下にて洗浄した。この湿ったケーキを、水（１．８７Ｌ、４．０Ｌ／ｋｇ）との撹拌下で洗浄し、次いでヘプタン（１．８７Ｌ、４．０Ｌ／ｋｇ）で洗浄した。生成物を、＋３０℃で真空下にて乾燥させて、化合物Ｎ（式中、Ａｒ^１は、ピリジニルである） ５３０ｇを、白色の結晶性固体として得た（９８％収率、９８．６ ＬＣ－Ａｒｅａ％純度、９９．８ｗ／ｗ％アッセイ）。
^１Ｈ ＮＭＲ（５００ＭＨｚ，ＤＭＳＯ－ｄ_６）δ ８．８１（ｄｄ，Ｊ＝１．２，５．１Ｈｚ，１Ｈ），８．１８（ｄｄｄ，Ｊ＝１．２，７．９，８．２Ｈｚ，１Ｈ），８．０８（ｄ，Ｊ＝７．９Ｈｚ，１Ｈ），７．７７（ｄｄ，Ｊ＝５．１，８．２Ｈｚ，１Ｈ），５．６８（ｍ，１Ｈ），５．０５（ｍ，２Ｈ），３．７０（ｍ，１Ｈ），２．２６（ｍ，１Ｈ），２．０５（ｍ，２Ｈ），１．０９（ｄ，Ｊ＝７．２Ｈｚ，３Ｈ），０．９８（ｄ，Ｊ＝７．２Ｈｚ，３Ｈ）．ＬＲＭＳ（ＥＳＩ）：Ｃ_１２Ｈ_１７Ｎ_１Ｓ_１＋Ｈについての計算値：２０８．３、実測値：２０８．３。ＩＲ（無溶媒）ｖｍａｘ ３０８６，２９８０，２９６６，２９３４，１４５０，１４２８，１３０４，１１０８，７９４，５９３，５４１。 Synthesis of compound N, where Ar ¹ is pyridinyl

2-(((2R,3S)-3-methylhex-5-en-2-yl)sulfonyl)pyridine (compound N, where Ar ¹ is pyridinyl): 10 L glass lined jacketed reactor was charged with compound M (wherein Ar ¹ is pyridinyl) (468 g, 2.26 mol, 1.00 eq) and the mixture was treated with methanol (1.4 L, 3.0 L/kg). Diluted. Acetic acid (136 g, 2.26 mol, 1.00 eq) was added followed by sodium tungstate dehydrate (75 g, 0.23 mol, 0.10 eq). The mixture was stirred at +25°C and hydrogen peroxide (276 g, 2.94 mol, 1.3 eq) was added over 4.5 hours while maintaining the temperature at NMT +25°C. After the addition was complete, the reaction was stirred for 24 hours. Water (2.34 L, 5.0 L/kg) was added over 1 hour to induce crystallization. The crystallization mixture was cooled to 0° C. and stirred for 2 hours. The product is then filtered off at 0° C. and the wet cake is then treated at +25° C. with aqueous sodium thiosulfate solution (1.2 mol/L solution; 1.87 L, 4.0 L/kg, 2.26 mol, 1.00 equivalents) under stirring. The wet cake was washed under agitation with water (1.87 L, 4.0 L/kg) and then with heptane (1.87 L, 4.0 L/kg). The product was dried under vacuum at +30° C. to give 530 g of compound N (wherein Ar ¹ is pyridinyl) as a white crystalline solid (98% yield, 98.6 LC - Area % purity, 99.8 w/w % assay).
¹ H NMR (500 MHz, DMSO-d ₆ ) δ 8.81 (dd, J=1.2, 5.1 Hz, 1 H), 8.18 (ddd, J=1.2, 7.9, 8.2 Hz , 1H), 8.08 (d, J = 7.9Hz, 1H), 7.77 (dd, J = 5.1, 8.2Hz, 1H), 5.68 (m, 1H), 5.05 (m, 2H), 3.70 (m, 1H), 2.26 (m, 1H), 2.05 (m, 2H), 1.09 (d, J=7.2Hz, 3H), 0. 98 (d, J=7.2Hz, 3H). LRMS ( _ESI ): calcd for _C12H17N1S1 +H _: 208.3, found: _208.3 . IR (solvent free) vmax 3086, 2980, 2966, 2934, 1450, 1428, 1304, 1108, 794, 593, 541.

（２Ｒ，３Ｓ）－３－メチルヘキサ－５－エン－２－スルホンアミド（化合物Ｚ）：１０Ｌのガラス裏地のジャケット付き反応器に、化合物Ｎ（式中、Ａｒ^１は、ピリジニルである）（３００ｇ、１．２５ｍｏｌ、１．００当量）及びナトリウムチオメトキシド（１０５ｇ、１．５０ｍｏｌ、１．２０当量）を充填した。脱気された溶媒であるｔｅｒｔ－ブチルメチルエーテル（３．３０Ｌ、１１．０Ｌ／ｋｇ）及びメタノール（３．００Ｌ、１．００Ｌ／ｋｇ）を添加し、得られた混合物を、ＨＰＬＣにより測定した場合に化合物Ｏの形成が完了するまで、１２時間にわたり＋３５℃で撹拌した。この反応物を＋２５℃まで冷却し、水（３．０Ｌ、１０Ｌ／ｋｇ）を添加した。相を分離し、水相を、ｔｅｒｔ－ブチルメチルエーテルで２回洗浄した（２×１．５Ｌ、２×５．０Ｌ／ｋｇ）。有機層を、廃棄した。生成物に富む水層に、＋２５℃で４時間にわたり空気をバブリングして、残留するナトリウムチオメトキシドを消費させた。水層を、ｔｅｒｔ－ブチルメチルエーテル（１．５Ｌ、５．０Ｌ／ｋｇ）で希釈した。この二相混合物に、酢酸ナトリウム三水和物（２００ｇ、１．５ｍｏｌ、１．２当量）及びヒドロキシルアミン－Ｏ－スルホン酸（１７０ｇ、１．５ｍｏｌ、１．２当量）を添加した。この二相混合物を、ＬＣにより測定した場合に生成物である化合物Ｚへのスルフィネートの変換が完了するまで、２時間にわたり＋２５℃で撹拌した。塩化ナトリウム水溶液（５．５ｍｏｌ／Ｌ溶液、１．３５Ｌ、４．５Ｌ／ｋｇ）を添加し、この混合物を３０分にわたり撹拌した。相を分離し、水層を、ｔｅｒｔ－ブチルメチルエーテルで２回抽出した（２×１．３５Ｌ、２×４．５０Ｌ／ｋｇ）。まとめた有機相を、炭酸水素ナトリウム水溶液（１ｍｏｌ／Ｌ溶液；９００ｍＬ、３．０Ｌ／ｋｇ）、塩化ナトリウム水溶液（５．５ｍｏｌ／Ｌ溶液、６００ｍＬ、２．０Ｌ／ｋｇ）、及び水（６００ｍＬ、２．０Ｌ／ｋｇ）で順次洗浄した。この有機相を、＋４０～４５℃で低真空下にて、総量６００ｍＬまで蒸留した。溶媒であるｔｅｒｔ－ブチルメチルエーテル（１．３５Ｌ、４．５０Ｌ／ｋｇ）を添加し、この混合物を、＋４０～＋４５℃で低真空下にて、総量６００ｍＬまで蒸留した。この溶液を、＋１５℃まで冷却し、ｎ－ヘプタン（１．５Ｌ、５．０Ｌ／ｋｇ）を２時間かけて緩やかに添加して、結晶化を促進させた。スラリーを、０℃まで冷却し、３時間にわたり撹拌した。この生成物をろ別し、湿ったケーキをｎ－ヘプタン（６００ｍＬ、２．０Ｌ／ｋｇ）で洗浄した。この生成物を、＋３０℃で真空下にて乾燥させて、化合物Ｚ １６８ｇを、白色の結晶性固体として得た（７６％収率、９９．８ ＬＣ－Ａｒｅａ％純度、９９．５％ＧＣ純度、１００．０ｗ／ｗ％アッセイ、９９．８％キラル－ＧＣ）。
^１Ｈ ＮＭＲ（５００ＭＨｚ，ＤＭＳＯ－ｄ_６）δ ６．６９（ｓ，２Ｈ），５．７５（ｍ，１Ｈ），５．０６（ｍ，２Ｈ），２．９２（ｍ，１Ｈ），２．３１（ｍ，１Ｈ），２．０３（ｍ，２Ｈ），１．１７（ｄ，Ｊ＝７．２Ｈｚ，３Ｈ），０．９２（ｄ，Ｊ＝７．２Ｈｚ，３Ｈ）．ＬＲＭＳ（ＥＳＩ）：Ｃ_７Ｈ_１５Ｎ_１Ｏ_２Ｓ_１＋Ｎａについての計算値：２００．１、実測値：２００．１。ＩＲ（無溶媒）ｖｍａｘ ３３２３，３２５５，２９８０，２９６２，１５５６，１４５２，１３１２，１１６５，１１１３７，９００，５９３，５４８，５１１。 Synthesis of compound Z

(2R,3S)-3-Methylhex-5-ene-2-sulfonamide (Compound Z): To a 10 L glass lined jacketed reactor was added 300 g of Compound N (where Ar ¹ is pyridinyl). , 1.25 mol, 1.00 eq) and sodium thiomethoxide (105 g, 1.50 mol, 1.20 eq) were charged. Degassed solvents tert-butyl methyl ether (3.30 L, 11.0 L/kg) and methanol (3.00 L, 1.00 L/kg) were added and the resulting mixture was measured by HPLC Stirred at +35° C. for 12 hours until formation of compound O was complete in some cases. The reaction was cooled to +25° C. and water (3.0 L, 10 L/kg) was added. The phases were separated and the aqueous phase was washed twice with tert-butyl methyl ether (2 x 1.5 L, 2 x 5.0 L/kg). The organic layer was discarded. Air was bubbled through the product-rich aqueous layer at +25° C. for 4 hours to consume residual sodium thiomethoxide. The aqueous layer was diluted with tert-butyl methyl ether (1.5L, 5.0L/kg). To this biphasic mixture was added sodium acetate trihydrate (200 g, 1.5 mol, 1.2 eq) and hydroxylamine-O-sulfonic acid (170 g, 1.5 mol, 1.2 eq). The biphasic mixture was stirred at +25° C. for 2 hours until complete conversion of the sulfinate to the product compound Z as determined by LC. Aqueous sodium chloride solution (5.5 mol/L solution, 1.35 L, 4.5 L/kg) was added and the mixture was stirred for 30 minutes. The phases were separated and the aqueous layer was extracted twice with tert-butyl methyl ether (2 x 1.35 L, 2 x 4.50 L/kg). The combined organic phases were combined with aqueous sodium bicarbonate solution (1 mol/L solution; 900 mL, 3.0 L/kg), aqueous sodium chloride solution (5.5 mol/L solution, 600 mL, 2.0 L/kg), and water (600 mL, 2.0 L/kg). The organic phase was distilled under low vacuum at +40-45° C. to a total volume of 600 mL. Solvent tert-butyl methyl ether (1.35 L, 4.50 L/kg) was added and the mixture was distilled under low vacuum at +40-+45° C. to a total volume of 600 mL. The solution was cooled to +15° C. and n-heptane (1.5 L, 5.0 L/kg) was slowly added over 2 hours to promote crystallization. The slurry was cooled to 0° C. and stirred for 3 hours. The product was filtered off and the wet cake was washed with n-heptane (600 mL, 2.0 L/kg). The product was dried under vacuum at +30° C. to give 168 g of compound Z as a white crystalline solid (76% yield, 99.8 LC-Area % purity, 99.5% GC purity , 100.0 w/w % assay, 99.8% chiral-GC).
¹ H NMR (500 MHz, DMSO-d ₆ ) δ 6.69 (s, 2H), 5.75 (m, 1H), 5.06 (m, 2H), 2.92 (m, 1H), 2. 31 (m, 1H), 2.03 (m, 2H), 1.17 (d, J=7.2Hz, 3H), 0.92 (d, J=7.2Hz, 3H). LRMS ( _ESI ): calcd for _{C7H15N1O2S1 +} Na: _200.1 , found: _200.1 . IR (solvent free) vmax 3323, 3255, 2980, 2962, 1556, 1452, 1312, 1165, 11137, 900, 593, 548, 511.

Claims (80)

Compound Z

Or a method for synthesizing a salt thereof,
(a) (2S,3S)-butane-2,3-diol, a bromide source, and acetic acid are mixed to form compound I

forming;
(b) compound I and a non-nucleophilic base are mixed to form compound J;

forming;
(c) compound J and an allyl nucleophile are mixed to form compound K;

forming;
(d) Compound K, a leaving group reagent, and an amine base are mixed to form Compound L;

(Wherein, LG is a leaving group)
forming;
(e) combining compound L, a non-nucleophilic base, and Ar ¹ —SH to form compound M;

(wherein Ar ¹ is a 5-12 membered heteroaryl containing 1-3 ring heteroatoms selected from O, N, and S)
forming;
(f) oxidizing compound M to compound N

forming;
and (g) combining compound N, a base, and hydroxylamine-O-sulfonic acid to form compound Z. 3. The method of claim 1, wherein the bromide source comprises HBr, _PBr3 , or combinations thereof. 3. The method of claim 2, wherein HBr is present in acetic acid in an amount of 20 w/w% to 50 w/w%. 4. The method of claim 3, wherein HBr is present as a 33 w/w% solution in acetic acid. A process according to any one of claims 1 to 4, wherein said mixing of step (a) is carried out at a temperature of -20°C to 10°C. The method of any one of claims 1-5, wherein said mixing of step (a) is carried out for 1 hour to 24 hours. 7. The method of claim 6, wherein said mixing of step (a) is performed for 15 hours to 20 hours. The method of any one of claims 1-7, wherein step (b) further comprises monoethylene glycol. 9. The method of claim 8, wherein for step (b), the non-nucleophilic base and monoethylene glycol are stirred together prior to mixing with compound I. The method of claim 9, wherein the non-nucleophilic base and monoethylene glycol are stirred together at a temperature of 25°C to 40°C. 11. The non-nucleophilic base of any one of claims 1-10, wherein the non-nucleophilic base comprises lithium tert-butoxide, sodium tert-butoxide, potassium tert-butoxide, sodium tert-amylate, potassium amylate, or combinations thereof. the method of. 12. The method of claim 11, wherein said non-nucleophilic base comprises potassium tert-butoxide. 13. Any one of claims 1-12, wherein said mixing of step (b) is performed in an organic solvent comprising tert-butyl methyl ether, 2-methyltetrahydrofuran, cyclopentyl methyl ether, dimethoxyethane, or combinations thereof. described method. 14. The method of claim 13, wherein the organic solvent comprises tert-butyl methyl ether. A method according to any one of claims 1 to 14, wherein said mixing of step (b) is carried out for 10 minutes to 2 hours. 16. The method of claim 15, wherein said mixing of step (b) is performed for 30 minutes. A process according to any one of the preceding claims, wherein said mixing of step (b) is performed at a temperature of 70°C to 120°C. The allyl nucleophile is

and X is a halide. 19. The method of claim 18, wherein X is Cl. of claims 1-19, wherein said mixing of step (c) is performed in an organic solvent comprising tetrahydrofuran, 2-methyltetrahydrofuran, tert-butylmethylether (MTBE), cyclopentylmethylether, dimethoxyethane, or combinations thereof. A method according to any one of paragraphs. 21. The method of claim 20, wherein the organic solvent comprises tetrahydrofuran and MTBE. The method of any one of claims 1-21, wherein compound J is added dropwise to said allyl nucleophile over a period of 1 hour to 5 hours. The method of any one of claims 1-22, wherein said mixing of step (c) is carried out for 1 hour to 6 hours. 24. The method of claim 23, wherein said mixing of step (c) is performed for 3 hours. A process according to any one of the preceding claims, wherein said mixing of step (c) is performed at a temperature of -20°C to 10°C. 26. The method of any one of claims 1-25, wherein compound J and said allyl nucleophile are present in a molar ratio of 1:1.05 to 1:3. The method of any one of claims 1-26, wherein the leaving group comprises F, Cl, Br, I, mesyl, tosyl, nosyl, or triflyl. 28. The method of claim 27, wherein said leaving group is mesyl. 29. The method of claim 27 or 28, wherein the leaving group reagent comprises mesyl chloride, tosyl chloride, nosyl chloride, methanesulfonic anhydride, paratoluenesulfonic anhydride, or combinations thereof. 30. The method of claim 29, wherein the leaving group reagent is mesyl chloride. The process of any one of claims 1-30, wherein said mixing of step (d) is performed in an organic solvent comprising dichloromethane, tetrahydrofuran, 2-methyltetrahydrofuran, tert-butyl methyl ether, or combinations thereof. . 32. The method of claim 31, wherein the organic solvent comprises tetrahydrofuran. 33. The method of claim 31 or 32, wherein the organic solvent does not contain dichloromethane. 34. The method of any one of claims 1-33, wherein the leaving group reagent is added to a solution comprising compound K and the amine base. 35. The method of claim 34, wherein the leaving group reagent is added to the solution over 2-3 hours and then stirred for 10 minutes-1 hour. Said amine bases of step (d) are trimethylamine, pyridine, triethylamine, aniline, diisopropylethylamine, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), 1,4-diazabicyclo[2. 2.2] octane (DABCO), 2,6-lutidine, or a combination thereof. 37. The method of claim 36, wherein said amine base comprises triethylamine. A process according to any one of the preceding claims, wherein said mixing of step (d) is performed at a temperature of -10°C to 10°C. 39. The method of any one of claims 1-38, wherein the leaving group is present in 1.2-2 molar equivalents relative to compound K. 40. The method of any one of claims 1-39, wherein the amine base is present in 1.8 to 3.3 molar equivalents, based on compound K. 41. The method of any one of claims 1-40, wherein for step (e), compound L is added to a mixture comprising Ar ¹ -SH and said non-nucleophilic base. 42. The method of claim 41, wherein Compound L is added dropwise over 3-6 hours. Said non-nucleophilic base of step (e) is lithium hexamethyldisilazide (“HMDS”), sodium HMDS, potassium HMDS, lithium diisopropylamide, sodium diisopropylamide, potassium diisopropylamide, lithium tert-butoxide, sodium tert- 43. The method of any one of claims 1-42, comprising butoxide, potassium tert-butoxide, lithium tert-amylate, sodium tert-amylate, potassium tert-amylate, or combinations thereof. 44. The method of claim 43, wherein the non-nucleophilic base comprises sodium tert-butoxide, potassium tert-butoxide, or sodium tert-amylate. 45. The method of any one of claims 1-44, wherein compound L and said non-nucleophilic base of step (e) are present in a molar ratio of 1:1.1 to 1:4. Ar ¹ is

46. The method of any one of claims 1-45, selected from the group consisting of Ar ¹ is

47. The method of claim 46, wherein 48. The method of any one of claims 1-47, wherein compound L and Ar ¹ -SH are present in a molar ratio of 1:1.05 to 1:2.5. 49. The method of any one of claims 1-48, wherein said mixing of step (e) of compound L, Ar ¹ -SH and non-nucleophilic base is carried out for 3-5 hours. A process according to any one of the preceding claims, wherein said mixing of step (e) is performed at a temperature of 60°C to 80°C. A process according to any one of the preceding claims, wherein prior to said oxidation of step (f), compound M is washed 3-5 times with aqueous sodium hydroxide. 52. The method of any one of claims 1-51, wherein the oxidation of step (f) comprises mixing compound M with an oxidation catalyst and hydrogen peroxide. 53. The method of claim 52, wherein the oxidation catalyst is sodium tungstate dehydrate, 3-chloroperbenzoic acid, or a combination thereof. 54. The method of claim 53, wherein the oxidation catalyst is sodium tungstate dehydrate. 55. The method of any one of claims 52-54, wherein compound M and said oxidation catalyst are present in a molar ratio of 1:0.05 to 1:0.5. 56. The method of any one of claims 52-55, wherein said oxidizing further comprises admixing acetic acid. 57. The method of any one of claims 52-56, wherein compound M and hydrogen peroxide are present in a molar ratio of 1:1.3 to 1:5. A method according to any one of claims 1 to 57, wherein said oxidation of step (f) is carried out in a solvent. 59. The method of claim 58, wherein the solvent comprises methanol or ethanol. 60. The method of any one of claims 52-59, wherein compound M, said oxidation catalyst, and acetic acid are mixed prior to adding hydrogen peroxide. 61. The method of claim 60, wherein hydrogen peroxide is added over a period of 3-5 hours. A method according to any one of the preceding claims, wherein said oxidation of step (f) is carried out at a temperature of 20°C to 25°C. With respect to step (g), compound N and said base are mixed together in a solvent to form intermediate compound O, prior to mixing with hydroxylamino-O-sulfuric acid.

(Where Q is an alkali metal cation)
63. The method of any one of claims 1-62, forming a 64. The method of claim 63, wherein said mixing of compound N and said base is performed in a solvent comprising tert-butyl methyl ether, methanol, tetrahydrofuran, 2-methyltetrahydrofuran, or combinations thereof. 65. The method of claim 64, wherein the solvent comprises tert-butyl methyl ether and methanol. 66. The method of any one of claims 63-65, wherein said mixing of compound N and said base is performed at a temperature of 25°C to 50°C. 67. The method of any one of claims 63-66, wherein the base comprises sodium thiomethoxide, sodium methoxide, methanol, and potassium carbonate, or combinations thereof. 68. The method of claim 67, wherein the base is sodium thiomethoxide. 69. The method of any one of claims 63-68, wherein hydroxylamine-O-sulfonic acid is added to said intermediate compound O along with sodium acetate, potassium acetate, sodium formate, potassium formate, or combinations thereof. . 70. The method of claim 69, wherein hydroxylamine-O-sulfonic acid is added to said intermediate compound O along with sodium acetate trihydrate. 4. The method of claim 1, wherein said mixing of said intermediate compound O, hydroxylamine-O-sulfonic acid, and sodium acetate is carried out in a solvent comprising tert-butyl methyl ether, methanol, tetrahydrofuran, 2-methyltetrahydrofuran, or combinations thereof. 70. The method according to 70. 72. The method of any one of claims 63-71, wherein said mixing of said intermediate compound O, hydroxylamine-O-sulfonic acid and sodium acetate is carried out for a period of 30 minutes to 4 hours. 73. The method of claim 72, wherein said mixing of said intermediate compound O, hydroxylamine-O-sulfonic acid, and sodium acetate is carried out for 2 hours. 74. The process of any one of claims 1-73, wherein said mixing of said intermediate compound O, hydroxylamine-O-sulfonic acid and sodium acetate is performed at a temperature between 25°C and 50°C. 75. The method of any one of claims 1-74, further comprising crystallizing compound Z. The crystallization comprises heating a solution of compound Z to 40° C.-45° C., then cooling the solution to 10° C.-15° C., and adding a crystallization solvent to the cooled solution to form compound Z. 76. The method of claim 75, comprising forming crystals of 77. The method of claim 76, wherein said solution of compound Z comprises tert-butyl methyl ether and said crystallization solvent comprises heptane. 77. The method of claim 76, wherein the solution of compound Z comprises methanol and the crystallization solvent comprises water. The method uses compound Z to form compound A1

or a salt or solvate thereof. The method uses compound Z to form compound A2

or a salt or solvate thereof.